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rs104895105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a familial mediterranean fever mutation
Make rs104895105(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position3247171
GeneMEFV
is asnp
is mentioned by
dbSNPrs104895105
dbSNP (classic)rs104895105
ClinGenrs104895105
ebirs104895105
HLIrs104895105
Exacrs104895105
Gnomadrs104895105
Varsomers104895105
LitVarrs104895105
Maprs104895105
PheGenIrs104895105
Biobankrs104895105
1000 genomesrs104895105
hgdprs104895105
ensemblrs104895105
geneviewrs104895105
scholarrs104895105
googlers104895105
pharmgkbrs104895105
gwascentralrs104895105
openSNPrs104895105
23andMers104895105
SNPshotrs104895105
SNPdbers104895105
MSV3drs104895105
GWAS Ctlgrs104895105
Max Magnitude3
OMIM608107
Desc
Variant0020
Relatedalso
ClinVar
Risk rs104895105(T;T)
Alt rs104895105(T;T)
Reference Rs104895105(C;C)
Significance Pathogenic
Disease Familial mediterranean fever Familial Mediterranean fever
Variation info
Gene MEFV
CLNDBN Familial mediterranean fever, autosomal dominant Familial Mediterranean fever
Reversed 1
HGVS NC_000016.9:g.3297171G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000002666.3, RCV000083696.1,